IL-4 inhibits mouse mast cell Fc epsilonRI expression through a STAT6-dependent mechanism

J Immunol. 1998 Dec 15;161(12):6915-23.

Abstract

Mast cell activation by IgE-mediated stimuli is a central event in atopic disease. The regulation of the mast cell high affinity receptor, Fc epsilonRI, is poorly understood. We show that IL-4 can inhibit Fc epsilonRI expression on mouse bone marrow-derived mast cells and fetal liver-derived mast cell progenitors. This effect could be observed at 2.5 ng/ml IL-4 and was dose dependent. IL-4-mediated inhibition of cultured BMMC required 4 days of stimulation and was sustained at maximum levels for at least 21 days. The inhibition of Fc epsilonRI expression resulted in decreased sensitivity to IgE-mediated stimulation, as measured by serotonin release, and the induction of mRNA for IL-4, IL-5, IL-6, and IL-13. Additionally, IL-4 could abrogate the IgE-mediated increase in Fc epsilonRI expression. Lastly, IL-4-mediated inhibition was dependent upon expression of the STAT6 transcription factor, as STAT6-deficient bone marrow-derived mast cells did not decrease Fc epsilonRI levels in response to IL-4. These data argue for a homeostatic role of IL-4 in the regulation of Fc epsilonRI expression, a role that could be critical to understanding atopic disease.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Animals
  • Bone Marrow Cells / drug effects
  • Bone Marrow Cells / metabolism
  • Cells, Cultured
  • Depression, Chemical
  • Gene Expression Regulation / drug effects*
  • Hypersensitivity, Immediate / immunology*
  • Interleukin-4 / pharmacology*
  • Interleukins / biosynthesis
  • Interleukins / genetics
  • Liver / cytology
  • Liver / embryology
  • Mast Cells / drug effects*
  • Mast Cells / metabolism
  • Mice
  • Mice, Inbred BALB C
  • Mice, Knockout
  • RNA, Messenger / biosynthesis
  • RNA, Messenger / genetics
  • Receptors, IgE / biosynthesis*
  • Receptors, IgE / genetics
  • STAT6 Transcription Factor
  • Serotonin / metabolism
  • Trans-Activators / deficiency
  • Trans-Activators / genetics
  • Trans-Activators / physiology*
  • Transcription, Genetic / drug effects*

Substances

  • Interleukins
  • RNA, Messenger
  • Receptors, IgE
  • STAT6 Transcription Factor
  • Stat6 protein, mouse
  • Trans-Activators
  • Interleukin-4
  • Serotonin